524713-66-4 Usage
Uses
Used in Coordination Chemistry:
2-(4-TERT-BUTYLPHENYL)PYRIDINE is used as a ligand for forming complexes with various metal ions. Its ability to coordinate with metals makes it a valuable component in the development of new coordination compounds with potential applications in catalysis, sensing, and other areas.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(4-TERT-BUTYLPHENYL)PYRIDINE is utilized as a building block for the synthesis of complex organic molecules. Its unique structure allows for the creation of a wide range of organic compounds with diverse properties and potential applications.
Used in Material Science:
2-(4-TERT-BUTYLPHENYL)PYRIDINE is employed in material science for the development of new materials with specific properties. Its incorporation into materials can lead to advancements in areas such as polymers, coatings, and other specialty materials.
Used in Pharmaceutical Production:
2-(4-TERT-BUTYLPHENYL)PYRIDINE is used as a key intermediate in the production of pharmaceuticals. Its unique structure and properties make it a promising candidate for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Production:
2-(4-TERT-BUTYLPHENYL)PYRIDINE is also used in the synthesis of agrochemicals, contributing to the development of new pesticides, herbicides, and other agricultural chemicals that can enhance crop protection and yield.
Used in Specialty Chemicals Production:
This versatile compound is utilized in the production of specialty chemicals, where its unique properties can be harnessed to create high-value products for various industries, such as fragrances, dyes, and other specialty applications.
Check Digit Verification of cas no
The CAS Registry Mumber 524713-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,7,1 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 524713-66:
(8*5)+(7*2)+(6*4)+(5*7)+(4*1)+(3*3)+(2*6)+(1*6)=144
144 % 10 = 4
So 524713-66-4 is a valid CAS Registry Number.
524713-66-4Relevant academic research and scientific papers
Reversible Concerted Metalation-Deprotonation C-H Bond Activation by [Cp*RhCl2]2
Vanderweide, Andrew I.,Brennessel, William W.,Jones, William D.
supporting information, p. 12960 - 12965 (2019/10/11)
The reversibility of the concerted metalation-deprotonation exchange of eight para-substituted phenylpyridines is examined with the parent Cp*RhCl(κ-C,N-NC5H4-C6H4). Equilibrium constants are determined, and the free energies are used to extract the most important parameters that control the thermodynamics. Keq values are found to correlate best with heterolytic C-H bond strengths but in a way that is not obvious considering the electrophilic nature of these activations.
Mild, visible light-mediated decarboxylation of aryl carboxylic acids to access aryl radicals
Candish,Freitag,Gensch,Glorius
, p. 3618 - 3622 (2017/07/11)
Herein we present the first example of aryl radical formation via the visible light-mediated decarboxylation of aryl carboxylic acids using photoredox catalysis. This method constitutes a mild protocol for the decarboxylation of cheap and abundant aryl carboxylic acids and tolerates both electron-rich substrates and those lacking ortho-substitution. The in situ formation of an acyl hypobromite is proposed to prevent unproductive hydrogen atom abstraction and trapping of the intermediate aroyloxy radical, enabling mild decarboxylation.
